Glenda Espinal

520 total citations
16 papers, 377 citations indexed

About

Glenda Espinal is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Glenda Espinal has authored 16 papers receiving a total of 377 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 7 papers in Cognitive Neuroscience. Recurrent topics in Glenda Espinal's work include Genetics and Neurodevelopmental Disorders (12 papers), Autism Spectrum Disorder Research (7 papers) and Mitochondrial Function and Pathology (3 papers). Glenda Espinal is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Autism Spectrum Disorder Research (7 papers) and Mitochondrial Function and Pathology (3 papers). Glenda Espinal collaborates with scholars based in United States, Thailand and Singapore. Glenda Espinal's co-authors include Paul J. Hagerman, Randi J. Hagerman, Flora Tassone, Isaac N. Pessah, Kyoungmi Kim, Craig H. Warden, Blythe Durbin‐Johnson, José R. López, Gaëlle Robin and Dalyir Pretto and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Annals of Neurology.

In The Last Decade

Glenda Espinal

16 papers receiving 374 citations

Peers

Glenda Espinal

GENET

CMN

Stephanie M. Kyle United States

Christie M. Buchovecky United States

Volker Endris Germany

Karim Hyder United States

Jussara Mendonça dos Santos Brazil

Danilo Bernardo United States

Susana R. Louros United Kingdom

Stephanie Newton United States

Marianna De Franceschi Italy

Giulia Sagona Italy

Stephanie M. Kyle United States

Glenda Espinal

334 ×1.2

GENET

307 ×1.3

150 ×0.9

37 ×0.7

CMN

38 ×1.2

Citations per year, relative to Glenda Espinal Glenda Espinal (= 1×) peers Stephanie M. Kyle

Countries citing papers authored by Glenda Espinal

Since Specialization

Citations

This map shows the geographic impact of Glenda Espinal's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Glenda Espinal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Glenda Espinal more than expected).

Fields of papers citing papers by Glenda Espinal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Glenda Espinal. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Glenda Espinal. The network helps show where Glenda Espinal may publish in the future.

Co-authorship network of co-authors of Glenda Espinal

This figure shows the co-authorship network connecting the top 25 collaborators of Glenda Espinal. A scholar is included among the top collaborators of Glenda Espinal based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Glenda Espinal. Glenda Espinal is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Hessl, David, Junyi Wang, Glenda Espinal, et al.. (2025). Longitudinal Analysis of Neuroradiological Biomarkers for Fragile X‐Associated Tremor/Ataxia Syndrome and Implications for Clinical Trials. Annals of Neurology. 98(3). 471–481. 1 indexed citations

Espinal, Glenda, Blythe Durbin‐Johnson, Andrea Schneider, et al.. (2024). FMR1 Protein Expression Correlates with Intelligence Quotient in Both Peripheral Blood Mononuclear Cells and Fibroblasts from Individuals with an FMR1 Mutation. Journal of Molecular Diagnostics. 26(6). 498–509. 2 indexed citations

Hessl, David, Emilio Ferrer, Glenda Espinal, et al.. (2023). FMR1 Carriers Report Executive Function Changes Prior to Fragile X‐Associated Tremor/Ataxia Syndrome: A Longitudinal Study. Movement Disorders. 39(3). 519–525. 3 indexed citations

Espinal, Glenda, Ramkumar Aishworiya, Andrea Schneider, et al.. (2022). Tophaceous gout of the nose in a male FMR1 premutation carrier. SHILAP Revista de lepidopterología. 10(11). e6586–e6586. 1 indexed citations

Hessl, David, Robert M. Miller, Glenda Espinal, et al.. (2022). The International Fragile X Premutation Registry: building a resource for research and clinical trial readiness. Journal of Medical Genetics. 59(12). 1165–1170. 2 indexed citations

Holm, Katharine Nichole, Anthony W. Herren, Sandra L. Taylor, et al.. (2021). Human Cerebral Cortex Proteome of Fragile X-Associated Tremor/Ataxia Syndrome. Frontiers in Molecular Biosciences. 7. 600840–600840. 12 indexed citations

Ma, Lisa, Anthony W. Herren, Glenda Espinal, et al.. (2019). Composition of the Intranuclear Inclusions of Fragile X-associated Tremor/Ataxia Syndrome. Acta Neuropathologica Communications. 7(1). 143–143. 52 indexed citations

Kim, Kyoungmi, David Hessl, Glenda Espinal, et al.. (2019). Association between IQ and FMR1 protein (FMRP) across the spectrum of CGG repeat expansions. PLoS ONE. 14(12). e0226811–e0226811. 56 indexed citations

Kumar, Madhur, et al.. (2017). Size and methylation mosaicism in males with Fragile X syndrome. Expert Review of Molecular Diagnostics. 17(11). 1023–1032. 46 indexed citations

10.

Robin, Gaëlle, José R. López, Glenda Espinal, et al.. (2017). Calcium dysregulation and Cdk5-ATM pathway involved in a mouse model of fragile X-associated tremor/ataxia syndrome. Human Molecular Genetics. 26(14). 2649–2666. 49 indexed citations

11.

Sweha, Stefan R., Blythe Durbin‐Johnson, Andrea Schneider, et al.. (2017). Clinical and molecular correlates in fragile X premutation females. eNeurologicalSci. 7. 49–56. 12 indexed citations

12.

Pretto, Dalyir, Carolyn M. Yrigollen, John B. Williamson, et al.. (2014). Clinical and molecular implications of mosaicism in FMR1 full mutations. Frontiers in Genetics. 5. 318–318. 78 indexed citations

13.

Chiu, Sally, et al.. (2009). Mouse hepatic lipase alleles with variable effects on lipoprotein composition and size. Journal of Lipid Research. 51(5). 1035–1048. 3 indexed citations

14.

Perroud, Bertrand, et al.. (2009). In vivo multiplex quantitative analysis of 3 forms of alpha melanocyte stimulating hormone in pituitary of prolyl endopeptidase deficient mice. Molecular Brain. 2(1). 14–14. 16 indexed citations

15.

Chiu, Sally, et al.. (2007). Identification of positional candidate genes for body weight and adiposity in subcongenic mice. Physiological Genomics. 31(1). 75–85. 28 indexed citations

16.

Chiu, Sally, Janis S. Fisler, Glenda Espinal, et al.. (2004). The Yellow Agouti Mutation Alters Some But Not All Responses to Diet and Exercise. Obesity Research. 12(8). 1243–1255. 16 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact